IQVIA is seeking a highly motivated Clinical Research Coordinator to join our team in Bengaluru, India. This full-time position offers an opportunity to contribute to cutting-edge clinical research while working alongside industry experts. The role involves conducting clinical procedures, ensuring compliance with Good Clinical Practice (GCP), and assisting investigators in managing clinical trials effectively.
Responsibilities in Job
As a Clinical Research Coordinator, your primary responsibilities will include:
- Providing research support to investigators to execute clinical studies.
- Reviewing study protocols, Case Report Forms (CRFs), and other study-specific documents.
- Attending relevant study meetings and maintaining regulatory documentation.
- Recruiting and screening patients for clinical trials.
- Designing and maintaining study-related source documentation.
- Conducting study visits, performing required procedures, and ensuring data accuracy.
- Handling lab testing, specimen collection, and logistics.
- Monitoring subject safety and reporting adverse reactions.
- Assisting in training new staff and maintaining training records.
- Preparing for study audits and regulatory inspections.
- Coordinating with research sites for staffing and scheduling research projects.
Qualifications Required
To be eligible for this position, candidates should meet the following qualifications:
- Bachelor’s Degree in a relevant field (preferred) or High School Diploma with relevant experience.
- Minimum 3 years of experience in a clinical environment or medical setting (e.g., medical assistant, assistant nurse, laboratory technician).
- Strong knowledge of clinical trial operations and regulatory compliance.
- Familiarity with Good Clinical Practices (GCP) and study-specific operating procedures.
- Ability to perform essential clinical procedures such as intravenous catheter insertion and spirometry testing.
- Applicable certifications and licenses as required by company or regulatory bodies.
Skills Required
The ideal candidate should possess the following skills:
- Excellent interpersonal and communication skills.
- Attention to detail and ability to maintain accuracy in clinical data.
- Proficiency in MS Windows and Office applications like Access, Outlook, and Word.
- Strong organizational skills with the ability to multitask in a fast-paced environment.
- Team player with the ability to collaborate effectively with investigators, managers, and research staff.
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